Literature DB >> 8096896

Blindness in offspring of women blinded by Leber's hereditary optic neuropathy.

D Mackey.   

Abstract

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Year:  1993        PMID： 8096896     DOI： 10.1016/0140-6736(93)91105-u

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  5 in total

1.  Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder.

Authors:  Gavin Hudson; Sharon Keers; Patrick Yu-Wai-Man; Philip Griffiths; Kirsi Huoponen; Marja-Liisa Savontaus; Eeva Nikoskelainen; Massimo Zeviani; Franco Carrara; Rita Horvath; Veronika Karcagi; Liesbeth Spruijt; I F M de Coo; Hubert J M Smeets; Patrick F Chinnery
Journal:  Am J Hum Genet       Date:  2005-10-11       Impact factor: 11.025

2.  No evidence for 'skewed' inactivation of the X-chromosome as cause of Leber's hereditary optic neuropathy in female carriers.

Authors:  R J Oostra; S Kemp; P A Bolhuis; E M Bleeker-Wagemakers
Journal:  Hum Genet       Date:  1996-04       Impact factor: 4.132

3.  Compensatory elevation of complex II activity in Leber's hereditary optic neuropathy.

Authors:  M Y Yen; H C Lee; J H Liu; Y H Wei
Journal:  Br J Ophthalmol       Date:  1996-01       Impact factor: 4.638

Review 4.  A review of primary hereditary optic neuropathies.

Authors:  M Votruba; S Aijaz; A T Moore
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

5.  Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees.

Authors:  N Howell; I Kubacka; S Halvorson; B Howell; D A McCullough; D Mackey
Journal:  Genetics       Date:  1995-05       Impact factor: 4.562
  5 in total

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